Canonical Allele Identifier: CA1148224335

Gene: MUTYH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45329405_45329406delinsGC , CM000663.2:g.45329405_45329406delinsGC	GRCh38
NC_000001.10:g.45795077_45795078delinsGC , CM000663.1:g.45795077_45795078delinsGC	GRCh37
NC_000001.9:g.45567664_45567665delinsGC	NCBI36
NG_008189.1:g.16065_16066delinsGC , LRG_220:g.16065_16066delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000412971.6:c.1082_1083delinsGC	ENSP00000410263.2:p.Cys361=
ENST00000435155.2:c.1499_1500delinsGC	ENSP00000403655.2:p.Cys500=
ENST00000467459.6:c.*328_*329delinsGC	ENSP00000435889.2:n.*328_*329delinsGC
ENST00000483127.2:c.1484_1485delinsGC	ENSP00000436469.2:p.Cys495=
ENST00000485271.6:c.*209_*210delinsGC	ENSP00000431264.2:n.*209_*210delinsGC
ENST00000529892.6:c.1319_1320delinsGC	ENSP00000432528.2:p.Cys440=
ENST00000533178.6:c.*795_*796delinsGC	ENSP00000436430.2:n.*795_*796delinsGC
ENST00000672314.2:c.1466_1467delinsGC	ENSP00000500828.2:p.Cys489=
ENST00000710952.2:c.1550_1551delinsGC MANE Plus Clinical	ENSP00000518552.2:p.Cys517=
ENST00000672818.3:c.1541_1542delinsGC	ENSP00000500891.1:p.Cys514=
ENST00000456914.7:c.1466_1467delinsGC MANE Select	ENSP00000407590.2:p.Cys489=
ENST00000671898.1:c.*209_*210delinsGC	ENSP00000499896.1:n.*209_*210delinsGC
ENST00000672011.1:c.*795_*796delinsGC	ENSP00000500418.1:n.*795_*796delinsGC
ENST00000672818.2:c.1541_1542delinsGC	ENSP00000500891.1:p.Cys514=
ENST00000354383.10:c.1469_1470delinsGC	ENSP00000346354.6:p.Cys490=
ENST00000355498.6:c.1466_1467delinsGC	ENSP00000347685.2:p.Cys489=
ENST00000372098.7:c.1541_1542delinsGC	ENSP00000361170.3:p.Cys514=
ENST00000372104.5:c.1466_1467delinsGC	ENSP00000361176.1:p.Cys489=
ENST00000372110.7:c.1511_1512delinsGC	ENSP00000361182.3:p.Cys504=
ENST00000372115.7:c.1508_1509delinsGC	ENSP00000361187.3:p.Cys503=
ENST00000448481.5:c.1499_1500delinsGC	ENSP00000409718.1:p.Cys500=
ENST00000450313.5:c.1550_1551delinsGC	ENSP00000408176.1:p.Cys517=
ENST00000456914.6:c.1466_1467delinsGC	ENSP00000407590.2:p.Cys489=
ENST00000467459.5:c.883_884delinsGC	ENSP00000435889.1:n.883_884delinsGC
ENST00000475516.5:c.*1279_*1280delinsGC	ENSP00000433843.1:n.*1279_*1280delinsGC
ENST00000481571.5:c.*1279_*1280delinsGC	ENSP00000436597.1:n.*1279_*1280delinsGC
ENST00000482094.5:n.787_788delinsGC
ENST00000485271.5:c.343_344delinsGC
ENST00000488731.6:c.551_552delinsGC	ENSP00000432330.1:p.Cys184=
ENST00000528013.6:c.1508_1509delinsGC	ENSP00000433130.2:p.Cys503=
ENST00000529892.5:c.541_542delinsGC
ENST00000529984.5:c.551_552delinsGC	ENSP00000437093.1:p.Cys184=
ENST00000531105.5:c.147_148delinsGC	ENSP00000431292.1:p.Val49=
ENST00000533178.5:c.1095_1096delinsGC	ENSP00000436430.1:n.1095_1096delinsGC
NM_001048171.1:c.1508_1509delinsGC	NP_001041636.1:p.Cys503=
NM_001048172.1:c.1469_1470delinsGC	NP_001041637.1:p.Cys490=
NM_001048173.1:c.1466_1467delinsGC	NP_001041638.1:p.Cys489=
NM_001048174.1:c.1466_1467delinsGC	NP_001041639.1:p.Cys489=
NM_001128425.1:c.1550_1551delinsGC , LRG_220t1:c.1550_1551delinsGC	NP_001121897.1:p.Cys517=
NM_001293190.1:c.1511_1512delinsGC	NP_001280119.1:p.Cys504=
NM_001293191.1:c.1499_1500delinsGC	NP_001280120.1:p.Cys500=
NM_001293192.1:c.1190_1191delinsGC	NP_001280121.1:p.Cys397=
NM_001293195.1:c.1466_1467delinsGC	NP_001280124.1:p.Cys489=
NM_001293196.1:c.1190_1191delinsGC	NP_001280125.1:p.Cys397=
NM_012222.2:c.1541_1542delinsGC	NP_036354.1:p.Cys514=
XM_011541497.1:c.1526_1527delinsGC	XP_011539799.1:p.Cys509=
XM_011541498.1:c.1508_1509delinsGC	XP_011539800.1:p.Cys503=
XM_011541499.1:c.1508_1509delinsGC	XP_011539801.1:p.Cys503=
XM_011541500.1:c.1508_1509delinsGC	XP_011539802.1:p.Cys503=
XM_011541501.1:c.1508_1509delinsGC	XP_011539803.1:p.Cys503=
XM_011541502.1:c.1508_1509delinsGC	XP_011539804.1:p.Cys503=
XM_011541503.1:c.1508_1509delinsGC	XP_011539805.1:p.Cys503=
XM_011541504.1:c.1499_1500delinsGC	XP_011539806.1:p.Cys500=
XM_011541505.1:c.1088_1089delinsGC	XP_011539807.1:p.Cys363=
XM_011541506.1:c.1088_1089delinsGC	XP_011539808.1:p.Cys363=
XM_011541507.1:c.1079_1080delinsGC	XP_011539809.1:p.Cys360=
XM_011541508.1:c.1094_1095delinsGC	XP_011539810.1:p.Cys365=
XR_946658.1:n.1777_1778delinsGC
NM_001350650.1:c.1121_1122delinsGC	NP_001337579.1:p.Cys374=
NM_001350651.1:c.1121_1122delinsGC	NP_001337580.1:p.Cys374=
NR_146882.1:n.1904_1905delinsGC
NR_146883.1:n.1718_1719delinsGC
XM_011541497.3:c.1526_1527delinsGC	XP_011539799.1:p.Cys509=
XM_011541500.3:c.1508_1509delinsGC	XP_011539802.1:p.Cys503=
XM_011541501.2:c.1508_1509delinsGC	XP_011539803.1:p.Cys503=
XM_011541502.2:c.1508_1509delinsGC	XP_011539804.1:p.Cys503=
XM_011541503.2:c.1508_1509delinsGC	XP_011539805.1:p.Cys503=
XM_011541504.2:c.1499_1500delinsGC	XP_011539806.1:p.Cys500=
XM_011541505.2:c.1088_1089delinsGC	XP_011539807.1:p.Cys363=
XM_011541506.2:c.1088_1089delinsGC	XP_011539808.1:p.Cys363=
XM_017001331.1:c.1508_1509delinsGC	XP_016856820.1:p.Cys503=
XM_017001332.1:c.1508_1509delinsGC	XP_016856821.1:p.Cys503=
XM_017001333.1:c.1508_1509delinsGC	XP_016856822.1:p.Cys503=
XM_017001334.1:c.1469_1470delinsGC	XP_016856823.1:p.Cys490=
XM_017001335.1:c.1190_1191delinsGC	XP_016856824.1:p.Cys397=
XM_017001336.1:c.1121_1122delinsGC	XP_016856825.1:p.Cys374=
XM_017001337.1:c.1121_1122delinsGC	XP_016856826.1:p.Cys374=
XM_024447244.1:c.1121_1122delinsGC	XP_024303012.1:p.Cys374=
XM_024447245.1:c.1121_1122delinsGC	XP_024303013.1:p.Cys374=
XM_024447248.1:c.1079_1080delinsGC	XP_024303016.1:p.Cys360=
XM_024447249.1:c.950_951delinsGC	XP_024303017.1:p.Cys317=
XM_024447250.1:c.950_951delinsGC	XP_024303018.1:p.Cys317=
XM_024447251.1:c.950_951delinsGC	XP_024303019.1:p.Cys317=
XR_001737190.1:n.1691_1692delinsGC
XR_001737192.1:n.1503_1504delinsGC
XR_002956643.1:n.1683_1684delinsGC
XR_002956644.1:n.2218_2219delinsGC
XR_946658.2:n.1791_1792delinsGC
NM_001048171.2:c.1466_1467delinsGC	NP_001041636.2:p.Cys489=
NM_001128425.2:c.1550_1551delinsGC MANE Plus Clinical	NP_001121897.1:p.Cys517=
NM_001048172.2:c.1469_1470delinsGC	NP_001041637.1:p.Cys490=
NM_001048173.2:c.1466_1467delinsGC	NP_001041638.1:p.Cys489=
NM_001048174.2:c.1466_1467delinsGC MANE Select	NP_001041639.1:p.Cys489=
NM_001293190.2:c.1511_1512delinsGC	NP_001280119.1:p.Cys504=
NM_001293191.2:c.1499_1500delinsGC	NP_001280120.1:p.Cys500=
NM_001293192.2:c.1190_1191delinsGC	NP_001280121.1:p.Cys397=
NM_001293195.2:c.1466_1467delinsGC	NP_001280124.1:p.Cys489=
NM_001293196.2:c.1190_1191delinsGC	NP_001280125.1:p.Cys397=
NM_001350650.2:c.1121_1122delinsGC	NP_001337579.1:p.Cys374=
NM_001350651.2:c.1121_1122delinsGC	NP_001337580.1:p.Cys374=
NM_012222.3:c.1541_1542delinsGC	NP_036354.1:p.Cys514=
NR_146882.2:n.1874_1875delinsGC
NR_146883.2:n.1723_1724delinsGC